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Literature summary for 3.5.4.5 extracted from

  • Sanchez-Quitian, Z.A.; Timmers, L.F.; Caceres, R.A.; Rehm, J.G.; Thompson, C.E.; Basso, L.A.; de Azevedo, W.F.; Santos, D.S.
    Crystal structure determination and dynamic studies of Mycobacterium tuberculosis cytidine deaminase in complex with products (2011), Arch. Biochem. Biophys., 509, 108-115.
    View publication on PubMed

Application

Application Comment Organism
drug development CDA is a target for development of specific enzyme inhibitors with potential anti-proliferative activity on cell growth of Mycobacterium tuberculosis, the major causative agent of tuberculosis Mycobacterium tuberculosis

Crystallization (Commentary)

Crystallization (Comment) Organism
purified CDA in complex with uridine and deoxyuridine, hanging drop vapor diffusion method, 0.002 ml of 12 mg/ml protein in 20 mM Tris-HCl pH 7.5 is mixed with 0.002 ml of reservoir solution containing 0.1 M HEPES, pH 7.5 and 4.3 M sodium chloride, ligands uridine and deoxyuridine are added by soaking method, X-ray diffractiuon structure determination and analysis at 2.4 and 1.9 A resolution,molecular dynamics simulation, structure modeling Mycobacterium tuberculosis

Organism

Organism UniProt Comment Textmining
Mycobacterium tuberculosis P9WPH3
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Mycobacterium tuberculosis H37Rv P9WPH3
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-

Subunits

Subunits Comment Organism
tetramer
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Mycobacterium tuberculosis

Synonyms

Synonyms Comment Organism
CDA
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Mycobacterium tuberculosis

General Information

General Information Comment Organism
metabolism cytidine deaminase is a key enzyme in the pyrimidine salvage pathway Mycobacterium tuberculosis
physiological function cytidine amidase is involved in the hydrolytic deamination of cytidine or 2'-deoxycytidine to uridine or 2'-deoxyuridine, determination of the protein-ligand recognition process, respectively Mycobacterium tuberculosis